Preparation of Amines

Which of the following reaction is involved in the preparation of primary amines:
(i) Hoffmann bromamide reaction and
(ii) Gabriel phthalimide synthesis

How will you convert benzene into $\mathrm{N},\mathrm{N}$-dimethylaniline?

Identify the final major product in the following reaction sequence.

$\mathrm{C}{\mathrm{H}}_3\mathrm{C}\mathrm{O}\mathrm{N}{\mathrm{H}}_2\stackrel{\mathrm{N}\mathrm{a}+\mathrm{R}\mathrm{O}\mathrm{H}}{\to }\mathrm{ }\mathrm{Z}+{\mathrm{H}}_2\mathrm{O}$ ; Z is

The source of nitrogen in Gabriel synthesis of amines is _____.(Potassium phthalimide/Potassium cyanide)

What is the product $\left(\mathrm{X}\right)$ in the given reaction?

What is the product $\left(\mathrm{X}\right)$ in the given reaction?

Acetanilide on nitration followed by alkaline hydrolysis mainly gives

Which of the following reactions will give a primary amine?

What is the product $\left(\mathrm{X}\right)$ in the given reaction?

The most suitable reagent for the conversion of $2-$phenylpropanamide into $1-$phenylethylamine is:-

Which of the following reagents would not be a good choice for reducing an aryl nitro compound to an amine?

Bromoethane reacts with ${\mathrm{NH}}_3$ to from:

Which one of the following gives secondary amine on reduction:

Ethanamide on Hoffman degradation produces _____.(Methanamine/Ethanamine)

The above reaction is conversion of Nitrobenzene to aniline. It is a _____ reaction for nitrobenzene as oxygen is removed.

Consider the following reaction,

${\mathrm{C}}_2{\mathrm{H}}_5\mathrm{Cl}+\mathrm{AgCN}\stackrel{\mathrm{EtOH}/{\mathrm{H}}_2\mathrm{O}}{⟶}\underset{¯}{\mathrm{X}}$ (major)

Which one of the following statements is true for $\underset{¯}{\mathrm{X}}?$

$\left(\mathrm{I}\right)$ It gives propionic acid on hydrolysis
$\left(\mathrm{II}\right)$ It has an ester functional group
$\left(\mathrm{III}\right)$ It has a nitrogen linked to ethyl carbon
$\left(\mathrm{IV}\right)$ It has a cyanide group